Canonical Allele Identifier: CA2638142646
Gene: PYY HGNC NCBI

Linked Data

gnomAD v4: 17-43952733-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43952733T>C , CM000679.2:g.43952733T>C GRCh38
NC_000017.10:g.42030101T>C , CM000679.1:g.42030101T>C GRCh37
NC_000017.9:g.39385627T>C NCBI36
NG_023338.1:g.56737A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000692052.1:c.*223A>G MANE Select ENSP00000509262.1:n.*223A>G
XM_011525035.1:c.*223A>G XP_011523337.1:n.*223A>G
NM_004160.5:c.*223A>G NP_004151.3:n.*223A>G
NM_001394028.1:c.*223A>G MANE Select NP_001380957.1:n.*223A>G
NM_001394029.1:c.*372A>G NP_001380958.1:n.*372A>G
NM_004160.6:c.*223A>G NP_004151.4:n.*223A>G
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